Related Books

OECD Guidelines for the Testing of Chemicals, Section 4 Test No. 482: Genetic Toxicology: DNA Damage and Repair, Unscheduled DNA Synthesis in Mammalian Cells in vitro
Language: en
Pages: 7
Authors: OECD
Categories:
Type: BOOK - Published: 1986-10-23 - Publisher: OECD Publishing

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The Test Guideline for Unscheduled DNA Synthesis (UDS) in mammalian cells in vitro describes procedures utilizing primary cultures, human lymphocytes or establi
Test No. 482: Genetic Toxicology: DNA Damage and Repair, Unscheduled DNA Synthesis in Mammalian Cells in Vitro
Language: en
Pages: 7
Authors: Organisation for Economic Co-operation and Development
Categories:
Type: BOOK - Published: 1986 - Publisher:

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Following the OECD Council decision, the Test Guideline 482 'Genetic Toxicology: DNA Damage and Repair, Unscheduled DNA Synthesis in Mammalian Cells in vitro' w
OECD Guidelines for the Testing of Chemicals, Section 4 Test No. 486: Unscheduled DNA Synthesis (UDS) Test with Mammalian Liver Cells in vivo
Language: en
Pages: 8
Authors: OECD
Categories:
Type: BOOK - Published: 1997-07-21 - Publisher: OECD Publishing

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The purpose of the unscheduled DNA synthesis (UDS) test with mammalian liver cells in vivo is to identify substances that induce DNA repair after excision and r
OECD Guidelines for the Testing of Chemicals, Section 4 Test No. 479: Genetic Toxicology: In vitro Sister Chromatid Exchange Assay in Mammalian Cells
Language: en
Pages: 5
Authors: OECD
Categories:
Type: BOOK - Published: 1986-10-23 - Publisher: OECD Publishing

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The sister chromatid exchange (SCE) assay is a short-term test for the detection of reciprocal exchanges of DNA between two sister chromatids of a duplicating c
Test No. 476: In Vitro Mammalian Cell Gene Mutation Tests using the Hprt and xprt genes
Language: en
Pages: 18
Authors: OECD
Categories:
Type: BOOK - Published: 2015-07-28 - Publisher: OECD Publishing

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The in vitro mammalian cell gene mutation test can be used to detect gene mutations induced by chemical substances. In this test, the used genetic endpoints mea